A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056282



Internal ID18798813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:46771152..46808270hg38UCSC Ensembl
Innerchr18:44351115..44388233hg19UCSC Ensembl
Innerchr18:42605113..42642231hg18UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3837119
hg1937119
hg1837119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565384
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056282
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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